Medicare Program; Virtual Meeting of the Medicare Evidence Development and Coverage Advisory Committee-July 22, 2020, 35933-35935 [2020-12720]
Download as PDF
Federal Register / Vol. 85, No. 114 / Friday, June 12, 2020 / Notices
35933
more tables designed to collect specific
information as detailed in Table 1.
TABLE 1—QUESTIONNAIRE DATA COLLECTION FORM DESIGN
Tab name
Description of data
Introduction .............
Terms ......................
Facility Details .........
Room Area ..............
EtO & EG Storage ..
Sterilizer Chambers
Aeration ...................
APCD Summary .....
APCD Details ..........
EtO Monitoring ........
Miscellaneous .........
Additional Info .........
Documents ..............
Introduction and instructions for completing and submitting the questionnaire.
Definitions or explanations of technical terms.
Information about facility registrations, ownership, general characteristics, facility-level data.
Characteristics, inventory of components, and control of individual room areas where EtO is used or emitted.
Questions regarding EtO storage in drums and containers, and ethylene glycol (EG) tanks.
Operation, monitoring, and control characteristics of sterilizer chambers, including chamber exhaust vents.
Details of aeration equipment.
Information about all air pollution control devices operated by the facility.
Details regarding air pollution control devices such as scrubbers, catalytic oxidizers, thermal oxidizers, and others.
Information about workspace monitoring, personal monitoring, room monitoring conducted by facility.
Questions regarding facility’s wastewater treatment and other items of EtO commercial sterilization operation.
Extra space to provide any additional information requested within the questionnaire.
Designated fields for reporter to attach documents requested throughout the questionnaire (e.g., facility diagram; process
flow diagrams; air permit; permit application documents; startup, shutdown, malfunction plan; EtO calculations and supporting information; performance tests; engineering tests; parametric monitoring; standard operating procedures; EtO
monitoring results; documentation of studies done on quantifying EtO residuals in your products; and other process and
instrumentation diagrams).
Reporter’s information and certification for completing and submitting the questionnaire.
jbell on DSKJLSW7X2PROD with NOTICES
Certification .............
As described in the instructions and
the questionnaire, facilities may claim
certain data as CBI in their response.
There is a cell in each worksheet to
indicate whether the worksheet contains
CBI and if so, each cell containing data
being claimed as CBI should be shaded
red. It should be noted that CAA section
114(c) exempts emissions data from
claims of confidentiality, and emissions
data provided may be made available to
the public. Emissions data should not be
marked confidential. A definition of
what the EPA considers emissions data
is provided in 40 CFR 2.301(a)(2)(i).
Facilities claiming CBI must submit
both a non-confidential and confidential
version of their response. All nonconfidential responses to the ICR would
be submitted to the EPA via email or on
a thumb drive, CD–ROM, or DVD
through the U.S. mail. All confidential
responses to the ICR would be
submitted on a thumb drive, CD–ROM,
or DVD to the EPA through the U.S.
mail. Non-confidential information
collected from this ICR will be made
available to the public. Any information
designated as confidential by an ICR
respondent that the EPA subsequently
determines to constitute CBI or a trade
secret under the EPA’s CBI regulations
at 40 CFR part 2, subpart B, will be
protected pursuant to those regulations
and, for trade secrets, under 18 U.S.C.
1905. If no claim of confidentiality
accompanies the information when it is
received by the EPA, it may be made
available to the public by the EPA
without further notice pursuant to the
EPA regulations at 40 CFR 2.203.
Form numbers: None.
VerDate Sep<11>2014
17:43 Jun 11, 2020
Jkt 250001
Respondents/affected entities:
Facilities subject to 40 CFR part 63,
subpart O.
Respondent’s obligation to respond:
Responses to the ICR are mandatory
under the authority of section 114 of the
CAA.
Estimated number of respondents: 66
(total).
Frequency of response: Once.
Total estimated burden: The
estimated cumulative respondent
burden is 6,201 hours. The estimated
cumulative Agency burden to
administer this ICR is 1,727 hours.
Burden is defined at 5 CFR 1320.03(b).
Total estimated cost: The estimated
cumulative costs to respondents is
$569,967, including $995 operation and
maintenance costs for media and
postage for submitting questionnaires
containing CBI. The estimated
cumulative Agency costs is $100,049
including $1,440 operation and
maintenance costs for data storage.
Dated: June 5, 2020.
Penny Lassiter,
Director, Sector Policies and Programs
Division.
[FR Doc. 2020–12728 Filed 6–11–20; 8:45 am]
BILLING CODE 6560–50–P
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3395–N]
Medicare Program; Virtual Meeting of
the Medicare Evidence Development
and Coverage Advisory Committee—
July 22, 2020
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces a
virtual public meeting of the Medicare
Evidence Development & Coverage
Advisory Committee (MEDCAC)
(‘‘Committee’’) will be held on
Wednesday, July 22, 2020. This meeting
will focus on the home use of
noninvasive positive pressure
ventilation in patients with chronic
respiratory failure (CRF) consequent to
chronic obstructive pulmonary disease
(COPD). We are seeking the MEDCAC’s
recommendations regarding the
characteristics that define those patient
selection and usage criteria,
concomitant services, and equipment
parameters necessary to best achieve
positive patient health outcomes in
beneficiaries with CRF consequent to
COPD. This meeting is open to the
public in accordance with the Federal
Advisory Committee Act (5 U.S.C. App.
2, section 10(a)).
DATES:
Meeting Date: The virtual meeting
will be held on Wednesday, July 22,
2020 from 8:00 a.m. until 4:30 p.m.,
Eastern Daylight Time (EDT).
SUMMARY:
E:\FR\FM\12JNN1.SGM
12JNN1
jbell on DSKJLSW7X2PROD with NOTICES
35934
Federal Register / Vol. 85, No. 114 / Friday, June 12, 2020 / Notices
Deadline for Submission of Written
Comments: Written comments must be
received at the email address specified
in the ADDRESSES section of this notice
by 5:00 p.m., Eastern Daylight Time
(EDT), on Monday, June 22, 2020. Once
submitted, all comments are final.
Deadlines for Speaker Registration
and Presentation Materials: The
deadline to register to be a speaker and
to submit PowerPoint presentation
materials and writings that will be used
in support of an oral presentation is 5:00
p.m., EDT, on Monday, June 22, 2020.
Speakers may register by phone or via
email by contacting the person listed in
the FOR FURTHER INFORMATION CONTACT
section of this notice. Presentation
materials must be received at the email
address specified in the ADDRESSES
section of this notice.
Submission of Presentations and
Comments: Presentation materials and
written comments that will be presented
at the meeting must be submitted via
email to MedCACpresentations@
cms.hhs.gov section of this notice by
Monday June 22, 2020.
Deadline for All Other Attendees
Registration: Individuals who want to
join the meeting may register online at
https://letsmeet.webex.com/letsmeet/
onstage/g.php?MTID=e6f9d4471a6f1f7
7e29f5c34c64ccdc4d by 11:59 p.m. EDT,
on Sunday, July 19, 2020.
Webinar and Teleconference Meeting
Information: Teleconference dial-in
instructions, and related webinar details
will be posted on the meeting agenda,
which will be available on the CMS
website https://www.cms.gov/medicarecoverage-database/indexes/medcacmeetingsindex.aspx?bc=BAAAAAAAAAAA&.
Participants in the MEDCAC meeting
will require the following: a computer,
laptop or smartphone where the WebEx
application needs to be downloaded; a
strong Wi-Fi or an internet connection
and access to use Chrome or Firefox
web browser and a webcam if the
meeting participant is scheduled to
speak or make a presentation during the
meeting.
Deadline for Submitting a Request for
Special Accommodations: Individuals
viewing or listening to the meeting who
are hearing or visually impaired and
have special requirements, or a
condition that requires special
assistance, should send an email to the
MEDCAC Coordinator as specified in
the FOR FURTHER INFORMATION CONTACT
section of this notice no later than 5:00
p.m., EDT on Friday, June 26, 2020.
ADDRESSES: Due to the current COVID–
19 public health emergency, the Panel
meeting will be held virtually.
VerDate Sep<11>2014
17:43 Jun 11, 2020
Jkt 250001
Tara
Hall, MEDCAC Coordinator, via email at
Tara.Hall@cms.hhs.gov or by phone
410–786–4347.
SUPPLEMENTARY INFORMATION:
FOR FURTHER INFORMATION CONTACT:
I. Background
MEDCAC, formerly known as the
Medicare Coverage Advisory Committee
(MCAC), is advisory in nature, with all
final coverage decisions resting with
CMS. MEDCAC is used to supplement
CMS’ internal expertise. Accordingly,
the advice rendered by the MEDCAC is
most useful when it results from a
process of full scientific inquiry and
thoughtful discussion, in an open
forum, with careful framing of
recommendations and clear
identification of the basis of those
recommendations. MEDCAC members
are valued for their background,
education, and expertise in a wide
variety of scientific, clinical, and other
related fields. (For more information on
MEDCAC, see the MEDCAC Charter
(https://www.cms.gov/Regulations-andGuidance/Guidance/FACA/Downloads/
medcaccharter.pdf) and the CMS
Guidance Document, Factors CMS
Considers in Referring Topics to the
MEDCAC (https://www.cms.gov/
medicare-coverage-database/details/
medicare-coverage-documentdetails.aspx?MCDId=10).
II. Meeting Topic and Format
This notice announces the
Wednesday, July 22, 2020, virtual
public meeting of the Committee. This
meeting will focus on the home use of
noninvasive positive pressure
ventilation in patients with CRF
consequent to COPD. Devices to be
considered are home mechanical
ventilators (HMVs), bi-level positive
airway pressure (BPAP) devices and
continuous positive airway pressure
(CPAP) devices. We are seeking the
MEDCAC’s recommendations regarding
the characteristics that define those
patient selection and usage criteria,
concomitant services, and equipment
parameters necessary to best achieve
positive patient health outcomes in
beneficiaries with CRF consequent to
COPD. The MEDCAC will specifically
focus on the scientific evidence
associated with the outcomes most
pertinent to the affected patient
population. Outcomes of interest will
include decreased mortality, decreased
frequency of exacerbations requiring ER
or hospital admission, increased time to
hospital re-admission for respiratory
related disease, and improved function
and quality of life.
Background information about this
topic, including panel materials, is
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
available at https://www.cms.gov/
medicare-coverage-database/indexes/
medcac-meetingsindex.aspx?bc=BAAAAAAAAAAA&.
Electronic copies of all the meeting
materials will be on the CMS website no
later than 2 business days before the
meeting. We encourage the participation
of organizations with expertise in the
appraisal of the state of evidence for the
use of HMV, BPAP, and CPAP
equipment in the home for the affected
patient population. This meeting is
open to the public. The Committee will
hear oral presentations from the public
for approximately 60 minutes. Time
allotted for each presentation may be
limited. If the number of registrants
requesting to speak is greater than what
can be reasonably accommodated
during the scheduled open public
hearing session, we may conduct a
lottery to determine the speakers for the
scheduled open public hearing session.
The contact person will notify
interested persons regarding their
request to speak by June 29, 2020. Your
comments must focus on issues specific
to the list of topics that we have
proposed to the Committee. The list of
research topics to be discussed at the
meeting will be available on the
following website prior to the meeting:
https://www.cms.gov/medicare-coveragedatabase/indexes/medcac-meetingsindex.aspx?bc=BAAAAAAAAAAA&.
We require that you declare at the
meeting whether you have any financial
involvement with manufacturers (or
their competitors) of any items or
services being discussed. Speakers
presenting at the MEDCAC meeting
must include a full disclosure slide as
their second slide in their presentation
for financial interests (for example, type
of financial association—consultant,
research support, advisory board, and
an indication of level, such as minor
association < $10,000 or major
association > $10,000) as well as
intellectual conflicts of interest (for
example, involvement in a federal or
nonfederal advisory committee that has
discussed the issue) that may pertain in
any way to the subject of this meeting.
If you are representing an organization,
we require that you also disclose
conflict of interest information for that
organization. If you do not have a
PowerPoint presentation, you will need
to present the full disclosure
information requested previously at the
beginning of your statement to the
Committee.
The Committee will deliberate openly
on the topics under consideration.
Interested persons may observe the
deliberations, but the Committee will
E:\FR\FM\12JNN1.SGM
12JNN1
35935
Federal Register / Vol. 85, No. 114 / Friday, June 12, 2020 / Notices
not hear further comments during this
time except at the request of the
chairperson. The Committee will also
allow a 15-minute unscheduled open
public session for any attendee to
address issues specific to the topics
under consideration. At the conclusion
of the day, the members will vote and
the Committee will make its
recommendation(s) to CMS.
III. Registration Instructions
CMS’ Coverage and Analysis Group is
coordinating meeting registration. While
there is no registration fee, individuals
must register to attend. You may register
online at https://www.cms.gov/apps/
events/upcomingevents.asp?strOrder
By=1&type=3 or by phone by contacting
the person listed in the FOR FURTHER
INFORMATION CONTACT section of this
notice by the deadline listed in the
DATES section of this notice. Please
provide your full name (as it appears on
your state-issued driver’s license),
address, organization, telephone
number(s), and email address. You will
receive a registration confirmation with
instructions for your participation at the
virtual public meeting.
IV. Collection of Information
This document does not impose
information collection requirements,
that is, reporting, recordkeeping or
third-party disclosure requirements.
Consequently, there is no need for
review by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995 (44
U.S.C. chapter 35).
The Acting Director for the Center for
Clinical Standards and Quality, at the
Centers for Medicare & Medicaid
Services, Jean Moody-Williams, having
reviewed and approved this document,
authorizes Evell J. Barco Holland, who
is the Federal Register Liaison, to
electronically sign this document for
purposes of publication in the Federal
Register.
Authority: 5 U.S.C. App. 2, section 10(a).
Dated: June 8, 2020.
Evell J. Barco Holland,
Federal Register Liaison, Department of
Health and Human Services.
[FR Doc. 2020–12720 Filed 6–10–20; 8:45 am]
BILLING CODE 4120–01–P
Families, Office of Planning, Research,
and Evaluation (OPRE), 330 C Street
SW, Washington, DC 20201, Attn: ACF
Reports Clearance Officer. All requests,
emailed or written, should be identified
by the title of the information collection.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Administration for Native
Americans (ANA) Ongoing Progress
Report (OPR) and Objective Work Plan
(OWP)
Administration for Native
Americans, Administration for Children
and Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families’ (ACF)
Administration for Native Americans
(ANA) is requesting a revision to the
information collection: Ongoing
Progress Report (OPR) and the Objective
Work Plan (OWP) (OMB #0970–0452).
Changes are proposed to reduce the
burden on the public by combining
ANA’s Annual Data Report (OMB
#0970–0475) with the OPR.
DATES: Comments due within 60 days of
publication. In compliance with the
requirements of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
ACF is soliciting public comment on the
specific aspects of the information
collection described above.
ADDRESSES: Copies of the proposed
collection of information can be
obtained and comments may be
forwarded by emailing infocollection@
acf.hhs.gov. Alternatively, copies can
also be obtained by writing to the
Administration for Children and
SUMMARY:
Description: Content changes are
being made to the currently approved
OPR. ANA will continue to use the
currently approved OPR with minimal
changes to the instructions for the
remainder of fiscal year (FY) 2020 and
will use the modified OPR beginning FY
2021. The modified OPR combines
ANA’s Annual Data Report (OMB
#0970–0475) with the OPR. The
information in the OPR is collected on
a semi-annual basis to monitor the
performance of grantees and better
gauge grantee progress.
The OPR information collection is
conducted in accordance with Sec. 811
[42 U.S.C. 2992] of the Native American
Programs Act and will allow ANA to
report quantifiable results across all
program areas. It also provides grantees
with parameters for reporting their
progress and helps ANA better monitor
and determine the effectiveness of their
projects.
There are no changes proposed to the
OWP. The OWP information collection
is conducted in accordance with 42
U.S.C. of the Native American Programs
Act of 1972, as amended. This
collection is necessary to evaluate
applications for financial assistance and
determine the relative merits of the
projects for which such assistance is
requested, as set forth in Sec. 806 [42
U.S.C. 2991d–1](a)(1).
Respondents: Federally and staterecognized tribes, Native Pacific
Islanders, Tribal Colleges and
Universities, native non-profits, and
consortia.
ANNUAL BURDEN ESTIMATES
Total number
of respondents
Instrument
Objective Work Plan ........................................................
Ongoing Progress Report FY 2020 .................................
Ongoing Progress Report FY 2021—Exp. Date .............
Total number of
responses
per respondent
300
200
200
Average
burden hours
per response
1
2
4
3
1
2
Total burden
hours
900
400
1600
Annual burden
hours *
300
133
533
jbell on DSKJLSW7X2PROD with NOTICES
* Burden is annualized over the three year approval period.
Estimated Total Annual Burden
Hours: 966.
Comments: The Department
specifically requests comments on (a)
whether the proposed collection of
information is necessary for the proper
VerDate Sep<11>2014
17:43 Jun 11, 2020
Jkt 250001
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) the quality, utility,
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
and clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
E:\FR\FM\12JNN1.SGM
12JNN1
Agencies
[Federal Register Volume 85, Number 114 (Friday, June 12, 2020)]
[Notices]
[Pages 35933-35935]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12720]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-3395-N]
Medicare Program; Virtual Meeting of the Medicare Evidence
Development and Coverage Advisory Committee--July 22, 2020
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces a virtual public meeting of the Medicare
Evidence Development & Coverage Advisory Committee (MEDCAC)
(``Committee'') will be held on Wednesday, July 22, 2020. This meeting
will focus on the home use of noninvasive positive pressure ventilation
in patients with chronic respiratory failure (CRF) consequent to
chronic obstructive pulmonary disease (COPD). We are seeking the
MEDCAC's recommendations regarding the characteristics that define
those patient selection and usage criteria, concomitant services, and
equipment parameters necessary to best achieve positive patient health
outcomes in beneficiaries with CRF consequent to COPD. This meeting is
open to the public in accordance with the Federal Advisory Committee
Act (5 U.S.C. App. 2, section 10(a)).
DATES:
Meeting Date: The virtual meeting will be held on Wednesday, July
22, 2020 from 8:00 a.m. until 4:30 p.m., Eastern Daylight Time (EDT).
[[Page 35934]]
Deadline for Submission of Written Comments: Written comments must
be received at the email address specified in the ADDRESSES section of
this notice by 5:00 p.m., Eastern Daylight Time (EDT), on Monday, June
22, 2020. Once submitted, all comments are final.
Deadlines for Speaker Registration and Presentation Materials: The
deadline to register to be a speaker and to submit PowerPoint
presentation materials and writings that will be used in support of an
oral presentation is 5:00 p.m., EDT, on Monday, June 22, 2020. Speakers
may register by phone or via email by contacting the person listed in
the FOR FURTHER INFORMATION CONTACT section of this notice.
Presentation materials must be received at the email address specified
in the ADDRESSES section of this notice.
Submission of Presentations and Comments: Presentation materials
and written comments that will be presented at the meeting must be
submitted via email to [email protected] section of this
notice by Monday June 22, 2020.
Deadline for All Other Attendees Registration: Individuals who want
to join the meeting may register online at https://letsmeet.webex.com/letsmeet/onstage/g.php?MTID=e6f9d4471a6f1f77e29f5c34c64ccdc4d by 11:59
p.m. EDT, on Sunday, July 19, 2020.
Webinar and Teleconference Meeting Information: Teleconference
dial-in instructions, and related webinar details will be posted on the
meeting agenda, which will be available on the CMS website https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&. Participants in the MEDCAC meeting will
require the following: a computer, laptop or smartphone where the WebEx
application needs to be downloaded; a strong Wi-Fi or an internet
connection and access to use Chrome or Firefox web browser and a webcam
if the meeting participant is scheduled to speak or make a presentation
during the meeting.
Deadline for Submitting a Request for Special Accommodations:
Individuals viewing or listening to the meeting who are hearing or
visually impaired and have special requirements, or a condition that
requires special assistance, should send an email to the MEDCAC
Coordinator as specified in the FOR FURTHER INFORMATION CONTACT section
of this notice no later than 5:00 p.m., EDT on Friday, June 26, 2020.
ADDRESSES: Due to the current COVID-19 public health emergency, the
Panel meeting will be held virtually.
FOR FURTHER INFORMATION CONTACT: Tara Hall, MEDCAC Coordinator, via
email at [email protected] or by phone 410-786-4347.
SUPPLEMENTARY INFORMATION:
I. Background
MEDCAC, formerly known as the Medicare Coverage Advisory Committee
(MCAC), is advisory in nature, with all final coverage decisions
resting with CMS. MEDCAC is used to supplement CMS' internal expertise.
Accordingly, the advice rendered by the MEDCAC is most useful when it
results from a process of full scientific inquiry and thoughtful
discussion, in an open forum, with careful framing of recommendations
and clear identification of the basis of those recommendations. MEDCAC
members are valued for their background, education, and expertise in a
wide variety of scientific, clinical, and other related fields. (For
more information on MEDCAC, see the MEDCAC Charter (https://www.cms.gov/Regulations-and-Guidance/Guidance/FACA/Downloads/medcaccharter.pdf) and
the CMS Guidance Document, Factors CMS Considers in Referring Topics to
the MEDCAC (https://www.cms.gov/medicare-coverage-database/details/medicare-coverage-document-details.aspx?MCDId=10).
II. Meeting Topic and Format
This notice announces the Wednesday, July 22, 2020, virtual public
meeting of the Committee. This meeting will focus on the home use of
noninvasive positive pressure ventilation in patients with CRF
consequent to COPD. Devices to be considered are home mechanical
ventilators (HMVs), bi-level positive airway pressure (BPAP) devices
and continuous positive airway pressure (CPAP) devices. We are seeking
the MEDCAC's recommendations regarding the characteristics that define
those patient selection and usage criteria, concomitant services, and
equipment parameters necessary to best achieve positive patient health
outcomes in beneficiaries with CRF consequent to COPD. The MEDCAC will
specifically focus on the scientific evidence associated with the
outcomes most pertinent to the affected patient population. Outcomes of
interest will include decreased mortality, decreased frequency of
exacerbations requiring ER or hospital admission, increased time to
hospital re-admission for respiratory related disease, and improved
function and quality of life.
Background information about this topic, including panel materials,
is available at https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&. Electronic copies of all
the meeting materials will be on the CMS website no later than 2
business days before the meeting. We encourage the participation of
organizations with expertise in the appraisal of the state of evidence
for the use of HMV, BPAP, and CPAP equipment in the home for the
affected patient population. This meeting is open to the public. The
Committee will hear oral presentations from the public for
approximately 60 minutes. Time allotted for each presentation may be
limited. If the number of registrants requesting to speak is greater
than what can be reasonably accommodated during the scheduled open
public hearing session, we may conduct a lottery to determine the
speakers for the scheduled open public hearing session. The contact
person will notify interested persons regarding their request to speak
by June 29, 2020. Your comments must focus on issues specific to the
list of topics that we have proposed to the Committee. The list of
research topics to be discussed at the meeting will be available on the
following website prior to the meeting: https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&.
We require that you declare at the meeting whether you have any
financial involvement with manufacturers (or their competitors) of any
items or services being discussed. Speakers presenting at the MEDCAC
meeting must include a full disclosure slide as their second slide in
their presentation for financial interests (for example, type of
financial association--consultant, research support, advisory board,
and an indication of level, such as minor association < $10,000 or
major association > $10,000) as well as intellectual conflicts of
interest (for example, involvement in a federal or nonfederal advisory
committee that has discussed the issue) that may pertain in any way to
the subject of this meeting. If you are representing an organization,
we require that you also disclose conflict of interest information for
that organization. If you do not have a PowerPoint presentation, you
will need to present the full disclosure information requested
previously at the beginning of your statement to the Committee.
The Committee will deliberate openly on the topics under
consideration. Interested persons may observe the deliberations, but
the Committee will
[[Page 35935]]
not hear further comments during this time except at the request of the
chairperson. The Committee will also allow a 15-minute unscheduled open
public session for any attendee to address issues specific to the
topics under consideration. At the conclusion of the day, the members
will vote and the Committee will make its recommendation(s) to CMS.
III. Registration Instructions
CMS' Coverage and Analysis Group is coordinating meeting
registration. While there is no registration fee, individuals must
register to attend. You may register online at https://www.cms.gov/apps/events/upcomingevents.asp?strOrderBy=1&type=3 or by phone by contacting
the person listed in the FOR FURTHER INFORMATION CONTACT section of
this notice by the deadline listed in the DATES section of this notice.
Please provide your full name (as it appears on your state-issued
driver's license), address, organization, telephone number(s), and
email address. You will receive a registration confirmation with
instructions for your participation at the virtual public meeting.
IV. Collection of Information
This document does not impose information collection requirements,
that is, reporting, recordkeeping or third-party disclosure
requirements. Consequently, there is no need for review by the Office
of Management and Budget under the authority of the Paperwork Reduction
Act of 1995 (44 U.S.C. chapter 35).
The Acting Director for the Center for Clinical Standards and
Quality, at the Centers for Medicare & Medicaid Services, Jean Moody-
Williams, having reviewed and approved this document, authorizes Evell
J. Barco Holland, who is the Federal Register Liaison, to
electronically sign this document for purposes of publication in the
Federal Register.
Authority: 5 U.S.C. App. 2, section 10(a).
Dated: June 8, 2020.
Evell J. Barco Holland,
Federal Register Liaison, Department of Health and Human Services.
[FR Doc. 2020-12720 Filed 6-10-20; 8:45 am]
BILLING CODE 4120-01-P